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EthSEQ: ethnicity annotation from whole exome sequencing data

SUMMARY: Whole exome sequencing (WES) is widely utilized both in translational cancer genomics studies and in the setting of precision medicine. Stratification of individual’s ethnicity is fundamental for the correct interpretation of personal genomic variation impact. We implemented EthSEQ to provi...

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Detalles Bibliográficos
Autores principales: Romanel, Alessandro, Zhang, Tuo, Elemento, Olivier, Demichelis, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818140/
https://www.ncbi.nlm.nih.gov/pubmed/28369222
http://dx.doi.org/10.1093/bioinformatics/btx165
Descripción
Sumario:SUMMARY: Whole exome sequencing (WES) is widely utilized both in translational cancer genomics studies and in the setting of precision medicine. Stratification of individual’s ethnicity is fundamental for the correct interpretation of personal genomic variation impact. We implemented EthSEQ to provide reliable and rapid ethnicity annotation from whole exome sequencing individual’s data, validated it on 1000 Genome Project and TCGA data (2700 samples) demonstrating high precision, and finally assessed computational performances compared to other tools. EthSEQ can be integrated into any WES based processing pipeline and exploits multi-core capabilities. AVAILABILITY AND IMPLEMENTATION: R package available at github.com/aromanel/EthSEQ and CRAN repository. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.